A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982193



Internal ID21891536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17897522..17897574hg38UCSC Ensembl
chr1:18224016..18224068hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982193
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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